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Liver Transplantation Prevents Progressive Neurological Impairment in Argininemia

Argininemia is a rare hereditary disease due to a deficiency of hepatic arginase, which is the last enzyme of the urea cycle and hydrolyzes arginine to ornithine and urea. The onset of the disease is usually in childhood, and clinical manifestations include progressive spastic paraparesis and mental...

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Main Authors: Silva, E. Santos, Cardoso, M. L., Vilarinho, L., Medina, M., Barbot, C., Martins, E.
Format: Artigo
Jezik:Inglês
Izdano: Springer Berlin Heidelberg 2013
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC3755545/
https://ncbi.nlm.nih.gov/pubmed/23559324
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/8904_2013_218
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